Input: Use your existing SomaScan® or Olink® proteomics datasets.
Output: Not just differential proteins — we quantify differential protein complexes and provide complex-level scores, statistics, and figures for publication.
Purpose: Transforms single-protein data into functional insights at the complex level.
Most cellular functions are executed not by individual proteins but by coordinated assemblies of interacting subunits, collectively known as protein complexes. Conventional proteomic approaches that measure proteins in isolation often overlook these cooperative interactions, leaving critical aspects of molecular regulation undiscovered. Direct analysis of protein complexes enables researchers to reveal regulatory mechanisms, pathway dynamics, and disease-associated molecular signatures that are invisible at the single-protein level. Profiling protein complexes therefore offers a more accurate and integrative understanding of how molecular networks function in both health and disease.
MetwareBio’s protein complex analysis service utilizes COMFIDENT (the COMplex FIngerprint DEconvolutioN Technology), a computational–experimental framework to quantify protein complexes on a large scale and reveal their dynamic behavior across biological conditions. COMFIDENT integrates two complementary data sources: a Complex Fingerprint Matrix (CFM) derived from high-throughput proteomic measurements of known complexes, and a Complex Connectivity Matrix (CCM) predicted from AI-based modeling of protein–protein interactions. By applying a likelihood-based statistical deconvolution algorithm, the method disentangles overlapping protein signals and infers the relative abundance of functional complexes across samples. This workflow enables precise quantification of both known and predicted protein assemblies, offering deeper insight into the cooperative nature of biological systems.
Workflow of COMFIDENT Protein Complex Quantification
Reveal Panels for Protein Complex Profiling
The Reveal Panels translate the power of COMFIDENT-based protein complex quantification into ready-to-use
solutions for large-scale proteomic studies. Together, these panels provide researchers with a flexible
platform to analyze both well-characterized and AI-predicted protein assemblies, enabling discovery across a
wide range of biological systems and disease contexts.
Reveal 2000
The Reveal 2000 Panel covers protein complexes that have been experimentally validated and functionally characterized in the literature. Each complex in this panel has known biological roles, making it ideal for studies focused on disease mechanisms, biomarker validation, and targeted pathway exploration.
Reveal 3000
The Reveal 3000 Panel integrates AI-predicted protein–protein interactions with experimental data, providing quantitative insight into previously uncharacterized complexes. It enables researchers to explore the broader protein interaction landscape, discover novel assemblies, and identify new molecular mechanisms underlying complex diseases.
The Reveal Panels offer extensive coverage and quantitative profiling of protein complexes across multiple proteomic platforms. By integrating both validated and AI-predicted complexes, they enable detection of over 3,000 protein assemblies measurable through commercial assays such as Olink and SomaLogic.
Reveal 2000 vs Reveal 3000—Protein Complex Coverage Across Olink & SomaScan
We offer a full-stack proteomics solution, enabling seamless integration of Olink and SomaScan proteomics data with protein complex quantification. This one-stop workflow ensures consistency across datasets and simplifies downstream biological interpretation.
Comprehensive Coverage of Known and Predicted Complexes
Our approach quantifies over 3,000 protein assemblies, spanning both experimentally validated and AI-predicted complexes. This broad coverage allows simultaneous investigation of established pathways and novel molecular interactions.
Quantitative and Reproducible Complex Profiling
By leveraging standardized workflows and rigorous statistical modeling, our platform provides reproducible and quantitative measurements of complex abundance across large cohorts, ensuring high data reliability and comparability.
Translational Insight from System-Level Analysis
Complex-level profiling reveals cooperative mechanisms and pathway dynamics that remain hidden at the single-protein level, enabling deeper understanding of disease mechanisms and therapeutic target networks.
Expert Support and Collaborative Flexibility
Our scientific team provides end-to-end project support—from study design to data interpretation—tailoring analysis strategies to your research objectives and existing proteomic data.
Data Requirements & Deliverables
We accept standardized quantitative proteomic data from Olink or SomaScan results with UniProt IDs and
protein abundance values—as input. The output includes quantified protein complex profiles with complex
names, subunit composition, and abundance scores. We can also provide summary plots, complex-protein
association analyses, and condition-based comparisons upon request, offering ready-to-use figures for
publication or presentation. Contact Us for Demo
Input— What You Provide
We accept quantitative protein expression data from from Olink and SomaScan assays. Each file should contain sample identifiers, UniProt accession IDs, and normalized abundance values for individual proteins. Example:
SampleID
UniProt
Level
Sample_01
P10145
6.650
Sample_01
P15692
8.079
Sample_01
P80098
3.329
...
...
...
Output— What You Receive
The analysis outputs quantitative scores for predicted and validated protein complexes across samples. Each result file provides complex names, constituent protein subunits (UniProt IDs), and complex-specific abundance or confidence scores. Example:
Complex
Subunits.UniProt
Sample1
FABP2-FABP6 complex
P12104;P51161
1.188
SORT1-THPO complex
Q99523;P40225
0.701
DECR1-THPO complex
Q16698;P40225
0.972
...
...
...
Applications of Protein Complex Analysis
Disease Mechanism and Pathway Discovery
Protein complex profiling helps reveal how molecular
assemblies reorganize in disease states. By quantifying complex-level changes, researchers can identify
disrupted signaling pathways and interaction networks that drive disease progression, offering new
insight into underlying molecular mechanisms.
Biomarker Identification and Precision Medicine
Complex-level biomarkers provide higher specificity than
single-protein markers, reflecting coordinated molecular activity rather than isolated abundance
changes. Such markers can improve early diagnosis, patient stratification, and treatment monitoring in
diverse conditions, including metabolic, cardiovascular, and inflammatory diseases.
Drug Target Discovery and Complex Dynamics
Many drug targets function within multi-protein complexes.
Protein complex analysis enables identification of target-associated assemblies and reveals how
compounds modulate these interactions, supporting rational drug design and mechanism-of-action studies.
Cancer Biology and Tumor Microenvironment
In oncology research, changes in protein complex composition
often underlie key processes such as signal transduction, immune evasion, and metastasis. Complex-level
quantification allows researchers to pinpoint cooperative protein networks that contribute to tumor
heterogeneity and therapeutic resistance.
Case Study: Protein Complex biomarkers for diseases (submitted & unpublished)
The results in the figure below demonstrate that the PLAUR-PLAU complex shows a significant difference in abundance between the control group and both the diabetes group and the calves pain group (N = 1,046). In contrast, individual components PLAUR and PLAU do not exhibit significant differences in abundance between the control group and the case groups. These findings suggest that the interaction between PLAUR and PLAU as a complex is more strongly associated with the tested conditions than the individual proteins alone. Meaning that the proteomic resources were not properly used to identify biomarkers.
PLAUR–PLAU Complex Outperforms Single Proteins in Disease Association
FAQ on Protein Complex Analysis
What types of input data are accepted?
We accept standardized quantitative proteomic data from platforms such as Olink or SomaScan. Each dataset should include sample identifiers, UniProt accession IDs, and normalized protein abundance values in .csv or .xlsx format.
What kind of results will I receive?
You will receive a comprehensive table of quantified protein complexes, including complex names, subunit UniProt IDs, and abundance or confidence scores for each sample. Optional summary plots and complex–protein association analyses can also be provided.
How many protein complexes can be quantified?
The analysis covers more than 3,000 known and AI-predicted protein assemblies, encompassing both experimentally validated complexes and computationally inferred interactions.
What is the minimum number of samples required?
There is no minimum sample requirement for compound-level analysis — a single sample is sufficient. For comparative designs (e.g., case vs. control), please determine the appropriate sample size based on your study design.
How long does the analysis take?
Results are delivered within 5 business days after your data submission is confirmed.
Have a project in mind? Tell us about your research, and our team will design a customized proteomics or metabolomics plan to support your goals. Ready to get started? Submit your inquiry or contact us at support-global@metwarebio.com.